# Are there racial/ethnic differences in antibiotic treatment of community acquired pneumonia in the inpatient setting?

**Authors:** Shana A. B. Burrowes, Mari-Lynn Drainoni, Tamar F. Barlam

PMC · DOI: 10.1371/journal.pone.0345788 · PLOS One · 2026-03-25

## TL;DR

The study found that non-Hispanic Black patients were more likely to receive appropriate antibiotic treatment for pneumonia in hospitals compared to non-Hispanic White patients, but treatment varied by hospital size and region.

## Contribution

The study identifies racial/ethnic disparities in antibiotic treatment for pneumonia and hospital-level factors influencing treatment consistency.

## Key findings

- Non-Hispanic Black patients had higher odds of receiving guideline-concordant antibiotic therapy compared to non-Hispanic White patients.
- Larger hospitals and those in the South and Northeast were less likely to provide guideline-concordant care.
- No significant link was found between treatment disparities and clinical outcomes.

## Abstract

Community Acquired Pneumonia (CAP) is the most common reason for antibiotic treatment in hospitalized adults. Some prior studies have found treatment differences by race/ethnicity, but research on the topic is limited, results are mixed, and it is unclear if clinical outcomes are affected.

We conducted a retrospective analysis of hospitalized patients >=18 years of age with a diagnosis of CAP from 2018–2021 across 457 US hospitals in the Vizient Inc. Clinical Data Base. We examined guideline concordant antibiotic treatment differences for inpatient CAP by patient race/ethnicity and hospital level factors and secondarily assessed whether treatment differences affect patient clinical outcomes.

There were 1,277,770 admissions. Over half of all patients received concordant antibiotic therapy. Non-Hispanic Black patients had an increased odds of receiving guideline concordant antibiotic care (OR 1.22 95% CI 1.21–1.23) compared to non-Hispanic White patients. As the number of hospital beds increased, the odds of receiving concordant therapy decreased, with the greatest reduced odds between hospitals with >500 beds vs < 75 beds (OR 0.68, 95% CI 0.66–0.70). As case mix index increased concordant care decreased with the lowest odds observed at hospitals with a case mix index >2 (OR 0.71 95% CI 0.7–0.72). Patients at hospitals in the South (OR 0.8 95% CI 0.79–0.81) and Northeast (OR 0.71, 95% CI 0.7–0.72) were less likely than those in the West to receive concordant care. There was no significant association between the interaction of race/ethnicity and receipt of guideline concordant therapy and clinical outcomes.

Non-Hispanic Black patients were more likely to received guideline-concordant care for CAP however significant differences in concordant therapy were seen at the hospital level. Understanding the interplay of race/ethnicity and concordant CAP therapy at the individual and population level is important for future research in the examination of disparities in care.

## Full-text entities

- **Diseases:** hypotension (MESH:D007022), pneumonia (MESH:D011014), death (MESH:D003643), aspiration pneumonia (MESH:D011015), C. difficile (MESH:D003015), infection (MESH:D007239), diabetes (MESH:D003920), anemia (MESH:D000740), rash (MESH:D005076), sepsis (MESH:D018805), chronic pulmonary disease (MESH:D002908), cerebrovascular disease (MESH:D002561), renal failure (MESH:D051437), thrombocytopenia (MESH:D013921), allergic reactions (MESH:D004342), COVID-19 (MESH:D000086382), MRSA (MESH:D013203), CAP (MESH:D003147), C. difficile enteritis (MESH:D004751), hypertension (MESH:D006973), Infectious (MESH:D003141), diarrhea (MESH:D003967)
- **Chemicals:** azithromycin (MESH:D017963), meropenem (MESH:D000077731), Methicillin (MESH:D008712), ampicillin + sulbactam (MESH:C035444), beta-lactam (MESH:D047090), cefepime (MESH:D000077723), ceftriaxone (MESH:D002443), ceftaroline (MESH:C490727), alcohol (MESH:D000438), cefotaxime (MESH:D002439), piperacillin/tazobactam (MESH:D000077725), vancomycin (MESH:D014640), fluoroquinolone (MESH:D024841), macrolide (MESH:D018942), imipenem/cilastatin (MESH:D000077728), doxycycline (MESH:D004318), ertapenem (MESH:D000077727), clarithromycin (MESH:D017291), levofloxacin (MESH:D064704), tigecycline (MESH:D000078304), linezolid (MESH:D000069349), moxifloxacin (MESH:D000077266)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Pseudomonas (RNA similarity group I, genus) [taxon 286], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC13016333/full.md

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Source: https://tomesphere.com/paper/PMC13016333